Ring stent

ABSTRACT

A wire stent assembly that has a first ring defining one end of the stent assembly, a second ring defining the second end of the stent assembly. Each ring is formed of wire. The wire of each ring also has a second section that extends parallel to the longitudinal axis of the wire stent assembly and perpendicular to the rings. Each of the rings has a loop that is parallel to the longitudinal axis and parallel to the rings. The stent assembly may form the support structure for a stent graft.

RELATED APPLICATIONS

The present patent document is a continuation of U.S. application Ser. No. 13/278,790, filed Oct. 21, 2011, which is a continuation of application Ser. No. 10/962,638, filed Oct. 12, 2004, now U.S. Pat. No. 8,043,357, which claims the benefit of the filing date under 35 U.S.C. §119(e) of Provisional U.S. Patent Application Ser. No. 60/510,242, filed Oct. 10, 2003. All of the foregoing applications are hereby incorporated by reference.

TECHNICAL FIELD

This invention relates to a medical device and in particular to a stent for endovascular and endoluminal vessel repair and support.

BACKGROUND OF THE INVENTION

Stents are used in surgical procedures to repair or support a body lumen. Stents may be balloon expandable or may be self expanding. That is, stents may be formed from a ductile material and be supplied in a contracted or reduced diameter form to enable deployment to a target lumen and then expanded to a larger diameter by the use of a balloon. In another form a stent may be formed from a resilient material and be supplied in a diametrically or radially constrained form for delivery and then expanded when radial constraint is removed. Such stents may be covered or uncovered.

Stents proposed by Gianturco (U.S. Pat. No. 5,035,706) have a closed zig zag configuration comprising struts and bends between the struts. These stents do not have good dimensional stability because when formed into a cylindrical stent, unless constrained, their diameter is not fixed. This means that in some situations, a stent may put more outwardly radial pressure on a vessel than is desirable or it may not be easy to seal a stent graft within such a cylindrical stent.

SUMMARY OF THE INVENTION

Stents are used in surgical procedures to repair or support a body lumen. Stents may be balloon expandable or may be self expanding. That is, stents may be formed from a ductile material and be supplied in a contracted or reduced diameter form to enable deployment to a target lumen and then expanded to a larger diameter by the use of a balloon. In another form a stent may be formed from a resilient material and be supplied in a diametrically or radially constrained form for delivery and then expanded when radial constraint is removed. Such stents may be covered or uncovered.

Stents proposed by Gianturco (U.S. Pat. No. 5,035,706) have a closed zig zag configuration comprising struts and bends between the struts. These stents do not have good dimensional stability because when formed into a cylindrical stent, unless constrained, their diameter is not fixed. This means that in some situations, a stent may put more outwardly radial pressure on a vessel than is desirable or it may not be easy to seal a stent graft within such a cylindrical stent.

SUMMARY OF THE INVENTION

In one illustrative and preferred embodiment therefore, the invention is said to reside in a stent arrangement comprising a first ring and a second ring, the second ring being substantially parallel to and spaced axially apart from the first ring and a plurality of zig zag portions extending between and around the peripheries of the first and second ring.

It is the object of this invention to provide a self expanding stent which has good dimensional stability.

All of the first ring, second ring and the zig zag portions can be from a portion of wire or a single piece of wire. Preferably the wire is a resilient wire.

Preferably each zig zag portion is formed by struts with a bend between adjacent struts. The bend in between the adjacent struts may include a helix arrangement to put more resiliency into each bend.

Alternatively each zig zag portion is formed by two struts with a bend, a circumferential portion and another bend between adjacent struts. In this arrangement the circumferential portion forms part of the respective ring which makes the attachment of the ring to a portion of graft material, as discussed below, more secure.

The bends between the struts may be adjacent the rings or incorporate one of the rings into the angle of the bend.

Preferably there are first and second turns of wire in each of the first ring and the second ring.

The terminal end of the wire in each of the first ring and the second ring is preferably provided with a loop so that the stent does not present a pointed end of wire which could damage a vessel.

Preferably the at least one ring is a first ring and adjacent alternate bends of the zig zag portion and a second ring is spaced apart from the first ring and adjacent an opposite bend of the zig zag portion and there are at least two turns of wire in the second ring and a terminal end of the wire in the second ring is provided with a loop so that the stent does not present a pointed end of wire which could damage a vessel.

In a preferred embodiment, the stent may be produced with first and second turns of the wire for the first ring, at least three zig zag pairs of struts extending around the periphery of the ring, a strut extending to the second ring and then at least three pairs of zig zag struts around the periphery of the second ring and extending back towards the first ring and then at least two turns of the wire for the second ring.

The wires are preferably made of stainless steel, nitinol or other resilient wire.

The stent, which when completed, is in a substantially cylindrical or drum form, may be covered or lined with a bio-compatible graft material or may be used un-lined.

The bio-compatible graft material can include polytetrafluoroethylene, Dacron, Thoralon™, polyamide or any other suitable biocompatible graft material.

While Dacron, expanded polytetrafluoroethylene (ePTFE), Thoralon™, or other synthetic biocompatible materials can be used for the tubular graft material for the stent graft, a naturally occurring biomaterial, such as collagen, is highly desirable, particularly a specially derived collagen material known as collagenous extracellular matrix (ECM) material, such as small intestinal submucosa (SIS). Besides SIS, examples of ECM's include pericardium, stomach submucosa, liver basement membrane, urinary bladder submucosa, tissue mucosa, and dura mater.

SIS is particularly useful, and can be made in the fashion described in Badylak et al., U.S. Pat. No. 4,902,508; Intestinal Collagen Layer described in U.S. Pat. No. 5,733,337 to Carr and in 17 Nature Biotechnology 1083 (November 1999); Cook et al., WIPO Publication WO 98/22158, dated 28 May 1998, which is the published application of PCT/US97/14855, the teachings of which are incorporated herein by reference. Irrespective of the origin of the material (synthetic versus naturally occurring), the material can be made thicker by making multilaminate constructs, for example SIS constructs as described in U.S. Pat. Nos. 5,968,096; 5,955,110; 5,885,619; and 5,711,969. In addition to xenogenic biomaterials, such as SIS, autologous tissue can be harvested as well, for use in forming the tubular graft material. Additionally Elastin or Elastin-Like Polypetides (ELPs) and the like offer potential as a material to fabricate the tubular graft material to form a device with exceptional biocompatibility.

SIS is available from Cook Biotech, West Lafayette, Ind., USA.

To assist with radial compressibility, each of the first and second rings may be made in a “wavy” form with the apices of the waves extending towards the other ring.

A stent according to this invention may be used at the ends of legs or arms of stent grafts to give dimensional stability where such arms or legs engage against the wall of a vessel. The stent can also be used as a short extension affixed to and extending from a fenestration in a stent graft to provide a good sealing and dimensionally stable surface for an extension arm from the fenestrated stent graft.

The stents according to this invention may be “piggy backed” or stacked with sequential rings and zig zags to make a longer tubular stent.

In one embodiment the rings and struts of the ring stent can be, for instance, laser cut from a metallic tube or cannula in a well known manner or commercially obtained from a number of stent manufacturers. The metal may be suitably heat treated to make it deformable and resilient.

The stents according to this invention may be manufactured in diameters of from 3 mm to 40 mm and lengths of from 3 mm to 40 mm. Preferably the diameter ranges from about half the length to twice the length and more preferably the diameter is about the same as the length.

The wire from which the stent in one form may be formed may have a diameter or thickness of from approximately 35 microns to approximately 500 microns. Where the stent is formed by laser cutting from a metal tube the diameter of the metal tube may have a diameter of from 3 mm to 40 mm and have a wall thickness of from about 35 microns to about 500 microns.

In a further form the invention may be said to reside in a stent arrangement comprising at least one of a first resilient ring and a second resilient ring, the second ring defining a plane which is substantially parallel to and spaced axially apart from the plane of the first ring and a plurality of zig zag portions extending between and around the periphery of a least one of the first ring and second ring.

Preferably at least one of the first ring and the second ring comprises a metallic material.

Preferably at least one of the first ring and the second ring is formed from a wire or a metal cannula.

The or each ring and the zig zag portions may be formed from a single piece of wire.

Each zig zag portion may be formed by struts with a bend between adjacent struts.

The bends between the struts may be adjacent the or each ring.

Preferably there are two turns of wire or metal cannula in each of the first ring and second ring.

A terminal end of the wire in the or each ring may be provided with a loop so that the stent does not present a pointed end of wire or metal cannula which could damage a vessel.

The at least one ring may be adjacent alternate bends of the zig zag portion and a second ring may be spaced apart from the first ring and in a parallel plane and adjacent the opposite bend of the zig zag portion.

In a further form, the invention is said to reside in a stent arrangement comprising first and second ring portions axially spaced apart and a plurality of zig zag portions between the first and second ring portions around the periphery thereof.

Preferably, each zig zag portion is formed by first and second struts with a bend in between them.

In a further form, the invention is said to reside in a stent formed from a single piece of resilient wire, the stent comprising, in order along the wire, at least one first circle or turn of the wire, a first set of zig zag struts around the periphery of the first turn wire, a strut to a position spaced axially from the first turn, a second set of zig zag struts around the periphery of the first turn and at least one second circle or turn of the wire.

The second circle or turn of wire is preferably substantially co-planar with the first circle or turn of wire.

In an alternative form the invention is said to reside in a stent arrangement comprising at least one ring formed from a portion of wire and a plurality of zig zag portions extending axially from and around the periphery of the ring.

The or each ring and the zig zag portions are preferably formed from a single piece of wire and each zig zag portion is formed by struts with a bend between adjacent struts. Preferably the bends between the struts are adjacent the or each ring.

In one embodiment there are two turns of wire in the or each ring. A terminal end of the wire in the or each ring may be provided with a loop so that the stent does not present a pointed end of wire which could damage a vessel.

In a further form the invention is said to reside in a stent arrangement comprising a first ring formed from a portion of wire, a second ring formed from a portion of wire, the second ring defining a plane which is substantially parallel to and spaced axially apart from the plane of the first ring and a plurality of struts extending between the first ring and the second ring around the periphery of the rings, each of the struts being angled to the axial direction of the ring.

Preferably the plurality of struts are formed from a continuous piece of material and the first and second rings are also formed from the continuous piece of material.

Preferably there are bends between adjacent struts or there is a bend, a circumferential portion extending around the respective ring and another bend between adjacent struts.

U.S. Pat. No. 5,387,235 entitled “Expandable Transluminal Graft Prosthesis For Repair Of Aneurysm” discloses apparatus and methods of retaining grafts onto deployment devices. These features and other features disclosed in U.S. Pat. No. 5,387,235 could be used with the present invention and the disclosure of U.S. Pat. No. 5,387,235 is herewith incorporated in its entirety into this specification.

U.S. Pat. No. 5,720,776 entitled “Barb and Expandable Transluminal Graft Prosthesis For Repair of Aneurysm” discloses improved barbs with various forms of mechanical attachment to a stent. These features and other features disclosed in U.S. Pat. No. 5,720,776 could be used with the present invention and the disclosure of U.S. Pat. No. 5,720,776 is herewith incorporated in its entirety into this specification.

U.S. Pat. No. 6,206,931 entitled “Graft Prosthesis Materials” discloses graft prosthesis materials and a method for implanting, transplanting replacing and repairing a part of a patient and particularly the manufacture and use of a purified, collagen based matrix structure removed from a submucosa tissue source. These features and other features disclosed in U.S. Pat. No. 6,206,931 could be used with the present invention and the disclosure of U.S. Pat. No. 6,206,931 is herewith incorporated in its entirety into this specification.

PCT Patent Publication No. WO 98/53761 entitled “A Prosthesis And A Method And Means Of Deploying A Prosthesis” discloses an introducer for a prosthesis which retains the prosthesis so that each end can be moved independently. These features and other features disclosed in PCT Patent Publication No. WO 98/53761 could be used with the present invention and the disclosure of PCT Patent Publication No. WO 98/53761 is herewith incorporated in its entirety into this specification.

U.S. Pat. No. 6,524,335 and PCT Patent Publication No. WO 99/29262 entitled “Endoluminal Aortic Stents” disclose a fenestrated prosthesis for placement where there are intersecting arteries. This feature and other features disclosed in U.S. Pat. No. 6,524,335 and PCT Patent Publication No. WO 99/29262 could be used with the present invention and the disclosure of U.S. Pat. No. 6,524,335 and PCT Patent Publication No. WO 99/29262 is herewith incorporated in its entirety into this specification.

U.S. patent application Ser. No. 10/280,486, filed Oct. 25, 2002 and published on May 8, 2003 as U.S. Patent Application Publication No. US 2003 0088305 A1 and PCT Patent Publication No. WO 03/034948 entitled “Prostheses For Curved Lumens” discloses prostheses with arrangements for bending the prosthesis for placement into curved lumens. This feature and other features disclosed in U.S. patent application Ser. No. 10/280,486, and U.S. Patent Application Publication No. US 2003 0088305 A1 and PCT Patent Publication No. WO 03/034948 could be used with the present invention and the disclosure of U.S. patent application Ser. No. 10/280,486, and U.S. Patent Application Publication No. US 2003 0088305 A1 and PCT Patent Publication No. WO 03/034948 is herewith incorporated in its entirety into this specification.

U.S. Provisional Patent Application Ser. No. 60/392,682, filed Jun. 28, 2002, and U.S. patent application Ser. No. 10/447,406, filed May 29, 2003, and Published on Dec. 18, 2003, as US Patent Application Publication No. US 2003 0233140 A1 entitled “Trigger Wires” disclose release wire systems for the release of stent grafts retained on introducer devices. This feature and other features disclosed in U.S. Provisional Patent Application Ser. No. 60/392,682 and U.S. patent application Ser. No. 10/447,406, filed May 29, 2003 could be used with the present invention and the disclosure of U.S. Provisional Patent Application Ser. No. 60/392,682 and U.S. patent application Ser. No. 10/447,406, filed May 29, 2003 are herewith incorporated in their entirety into this specification.

U.S. Provisional Patent Application Ser. No. 60/392,667, filed Jun. 28, 2002, and U.S. patent application Ser. No. 10/609,846, filed Jun. 30, 2003, and Published on May 20, 2004, as US Patent Application Publication No. US 2004 0098079 A2, and PCT Patent Publication No. WO 2004/028399 entitled “Thoracic Deployment Device” disclose introducer devices adapted for deployment of stent grafts particularly in the thoracic arch. This feature and other features disclosed in U.S. Provisional Patent Application Ser. No. 60/392,667, U.S. patent application Ser. No. 10/609,846, and US Patent Application Publication No. US 2004 0098079 A1, and PCT Patent Publication No. WO 2004/028399 could be used with the present invention and the disclosure of U.S. Provisional Patent Application Ser. No. 60/392,667, U.S. patent application Ser. No. 10/609,846, and US Patent Application Publication No. US 2004 0098079 A1, and PCT Patent Publication No. WO 2004/028399 is herewith incorporated in its entirety into this specification.

U.S. Provisional Patent Application Ser. No. 60/392,599, filed Jun. 28, 2002, and U.S. patent application Ser. No. 10/609,835, filed Jun. 30, 2003, and published on Jun. 3, 2004, as U.S. Patent Application Publication No. US 2004 0106978 A1, and PCT Patent Publication No. WO 2004/002370 entitled “Thoracic Aortic Aneurysm Stent Graft” disclose stent grafts that are useful in treating aortic aneurysms particularly in the thoracic arch. This feature and other features disclosed in U.S. Provisional Patent Application Ser. No. 60/392,599, U.S. patent application Ser. No. 10/609,835, and U.S. Patent Application Publication No. US 2004 0106978 A1, and PCT Patent Publication No. WO 2004/002370 could be used with the present invention, and the disclosure of U.S. Provisional Patent Application Ser. No 60/392,599, U.S. patent application Ser. No. 10/609,835, and U.S. Patent Application Publication No. US 2004 0106978 A1, and PCT Patent Publication No. WO 2004/002370 is herewith incorporated in its entirety into this specification.

U.S. Provisional Patent Application Ser. No. 60/391,737, filed Jun. 26, 2002, U.S. patent application Ser. No. 10/602,930, filed Jun. 24, 2003, and published on Mar. 18, 2004, as U.S. Patent Application Publication No. US 2004 0054396 A1, and PCT Patent Publication No. WO 2004/002365 entitled “Stent-Graft Fastening” disclose arrangements for fastening stents onto grafts particularly for exposed stents. This feature and other features disclosed in U.S. Provisional Patent Application No. 60/391,737, U.S. patent application Ser. No. 10/602,930, and U.S. Patent Application Publication No. US 2004 0054396 A1, and PCT Patent Publication No. WO 2004/002365 could be used with the present invention and the disclosure of U.S. Provisional Patent Application Ser. No. 60/391,73, U.S. patent application Ser. No. 10/602,930, and U.S. Patent Application Publication No. US 2004 0054396 A1, and PCT Patent Publication No. WO 2004/002365 is herewith incorporated in its entirety into this specification.

U.S. Provisional Patent Application Ser. No. 60/405,367, filed Aug. 23, 2002, U.S. patent application Ser. No. 10/647,642, filed Aug. 25, 2003, and published on Apr. 15, 2004, as U.S. Patent Application Publication No. US 2004 0073289 A1, and PCT Patent Publication No. WO 2004/017868 entitled “Asymmetric Stent Graft Attachment” disclose retention arrangements for retaining onto and releasing prostheses from introducer devices. This feature and other features disclosed in U.S. Provisional Patent Application Ser. No. 60/405,367, filed Aug. 23, 2002, U.S. patent application Ser. No. 10/647,642, filed Aug. 25, 2003, and U.S. Patent Application Publication No. US 2004 0073289 A1, and PCT Patent Publication No. WO 2004/017868 could be used with the present invention and the disclosure of U.S. Provisional Patent Application Ser. No. 60/405,367, filed Aug. 23, 2002, U.S. patent application Ser. No. 10/647,642, filed Aug. 25, 2003, and U.S. Patent Application Publication No. US 2004 0073289 A1, and PCT Patent Publication No. WO 2004/017868 is herewith incorporated in its entirety into this specification.

U.S. patent application Ser. No. 10/322,862, filed Dec. 18, 2002 and published as Publication No. US2003-0120332, and PCT Patent Publication No. WO03/053287 entitled “Stent Graft With Improved Adhesion” disclose arrangements on stent grafts for enhancing the adhesion of such stent grafts into walls of vessels in which they are deployed. This feature and other features disclosed in U.S. patent application Ser. No. 10/322,862, filed Dec. 18, 2002 and published as Publication No. US2003-0120332, and PCT Patent Publication No. WO03/053287 could be used with the present invention and the disclosure of U.S. patent application Ser. No. 10/322,862, filed Dec. 18, 2002 and published as Publication No. US2003-0120332, and PCT Patent Publication No. WO03/053287 are herewith incorporated in its entirety into this specification.

U.S. Provisional Patent Application Ser. No. 60/405,769, filed Aug. 23, 2002, U.S. patent application Ser. No. 10/645,095, filed Aug. 23, 2003, and published on Apr. 29, 2004, as U.S. Patent Application Publication No. US 2004 0082990 A1, and PCT Patent Publication No. WO 2004/017867 entitled “Composite Prostheses” discloses prostheses or stent grafts suitable for endoluminal deployment. These prostheses and other features disclosed in U.S. Provisional Patent Application Ser. No. 60/405,769, U.S. patent application Ser. No. 10/645,095, and U.S. Patent Application Publication No. US 2004 0082990 A1, and PCT Patent Publication No. WO 2004/017867 could be used with the present invention and the disclosure of U.S. Provisional Patent Application Ser. No. 60/405,769, U.S. patent application Ser. No. 10/645,095, and U.S. Patent Application Publication No. US 2004 0082990 A1, and PCT Patent Publication No. WO 2004/017867 is herewith incorporated in its entirety into this specification.

BRIEF DESCRIPTION OF THE DRAWINGS

This then generally describes the invention but to assist at understanding, reference will now be made to the accompanying drawings which show some preferred embodiments of the invention.

In the drawings:

FIG. 1 shows a perspective view of a first embodiment of stent according to this invention;

FIG. 2 shows the stent of the embodiment of FIG. 1 with an internal covering of a biocompatible graft material;

FIG. 3 shows the stent of the embodiment of FIG. 1 with an external covering of a biocompatible graft material;

FIG. 4 shows an alternative embodiment of a stent according to this embodiment;

FIG. 5 shows a still further embodiment of a stent according to this invention;

FIG. 6 shows a plan view of a stent according to this invention;

FIG. 7 shows a side elevation of a stent according to this invention;

FIG. 8 shows an embodiment of a stacked stent according to this invention;

FIG. 9 shows an embodiment of this invention used as a stent on the end of a leg of a bifurcated stent graft;

FIG. 10 shows a perspective view of a alternative embodiment of the invention;

FIG. 11 shows a developed view of a further alternative embodiment of the invention;

FIG. 12 shows a perspective view of the alternative embodiment of the invention shown in FIG. 11;

FIG. 13 shows a perspective view of the alternative embodiment of the invention; and

FIG. 14 shows a perspective view of the further embodiment of the invention.

DETAILED DESCRIPTION OF THE DRAWINGS AND THE PRESENTLY PREFERRED EMBODIMENTS

Now looking more closely at the drawings and in particular FIG. 1, it will be seen that the stent 1 according to one embodiment of this invention comprises a first resilient ring assembly 3 and a second resilient ring assembly 4 spaced (preferably parallel) to and axially away from the first ring assembly 3 and a number of zig zag struts 5 between the first resilient ring assembly 3 and the second resilient ring assembly 4. The first and second resilient ring assemblies and the struts comprise a metallic wire.

Although metal or metal alloy materials are preferred other resilient materials such as polymers, carbon fibres and other biocompatible materials are also contemplated.

The first ring assembly 3 commences at a loop 7 of the wire and is formed from two circles or turns of wire 9 and then at 11 there is a bend and the wire is angled in a first strut 13 extending to a bend 15 adjacent the second ring assembly 4 and then a further angled strut 17 to a bend 19 adjacent the first ring assembly 3. Consecutive angled struts and bends extend around the periphery of the ring assembly 3 and the ring assembly 4 from the bend 19 until bend 21 adjacent to the bend 11 where there is an axial strut 23 extending to the second ring assembly 4 and a bend 25. From the bend 25 is an angled strut 27 which extends to the first ring assembly 3 where there is a bend 29 and a subsequent angled strut 31. Subsequent angled struts and bends extend around the periphery of the second ring assembly 4 and first the ring assembly 3 from strut 31 to a bend 33 adjacent to bend 25 where the wire extends to a first circle or turn 35 of the ring assembly 4 and then to a second turn 37 of the ring assembly 4 to finally terminate in a loop 39 of the wire.

The wire in this embodiment is preferably nitinol and has a diameter of 150 microns and the stent has a diameter of 8 mm and a length of 9 mm. There are three sets of struts with a bend between them extending from each of the rings to the other of the rings giving a total of twelve angled struts and one axial strut.

By this arrangement a stent with good radial dimensional stability is formed because the rings restrict radial expansion and contraction but being formed from resilient wire has good compressibility to enable it to be deployed endoluminally in a contracted state.

FIG. 2 shows an embodiment of the stent shown in FIG. 1 with a biocompatible graft material lining. The graft material 40 is retained by stitching 41 to the first ring assembly 3 and by stitching 42 to the second ring assembly 4. Stitching 44 is also provided to retain the graft material into a cylindrical shape where the struts cross between the first and second rings. By this arrangement a portion of stent graft is formed which has good dimensional stability and which may be mounted to or provided on the end of a stent graft, on the leg of a stent graft, or as or on a side arm from a stent g raft.

The graft material may be Dacron, Thoralon™ material, nylon or any other suitable material such as collagenous extracellular matrix (ECM) material including small intestine submucosa, which is commercially available from Cook Biotech, West Lafayette, Ind., USA.

Similarly in FIG. 3 a biocompatible graft material covering 50 is provided on the outside of the stent 1 with the material 50 sewn to and retained onto the first ring assembly 3 by stitching 51, onto the second ring assembly 4 by stitching 52 and to the struts by stitching 53.

FIG. 4 shows a further embodiment of a stent according to this invention. In this embodiment the first ring 60 and the second ring 61 of the stent are formed as a wavy ring with the waves extending axially so that there are alternate troughs 62 and crests 63. The crests 63 correspond substantially with the bends 64 between struts 65 of the zig zag portion 66 of the stent. The apices 62 extend towards the ring 61

The wavy rings can be formed so that their rest diameter is substantially the desired final diameter of the stent.

These wavy rings, while still providing good dimensional stability, allow radial compression of the rings 60 and 61 as well as the zig zag portion 66. This will assist with enabling this form of the stent to be radially compressed onto a delivery device as required.

FIG. 5 shows a still further embodiment of a stent according to this invention. In this embodiment, the stent has a two-circle or turn ring 70 of wire at its upper end, a two-circle or turn ring 72 of wire at its lower end and a number of zig zag struts 74 of wire between the rings 70 and 72. In this embodiment, however, all of the pairs of struts commence at the ring 70 and after six pairs of zig zag struts, a single strut 76 extends to the ring 72 to complete the stent with the two turns of the second ring. Rather than the axial strut 76 there may be a further angled strut between the first ring 70 and the second ring 72. In this embodiment the bends 73 incorporate the ring 70 within the acute angle of the bend and the bends 75 incorporate the ring 72 within the acute angle of the bend.

FIG. 6 shows a plan view of the stent shown in FIG. 1 and it will be noted that the stent in plan view is substantially cylindrical and the ring 3 and the termination loops 7 and 39 can be seen.

FIG. 7 shows a side elevation view of the stent similar to that shown in FIG. 1 except that at the apex of each of the bends there is a helix arrangement 38 to give more resilience to each bend. It will be noted that the zig zag struts 5 provide an essentially cylindrical peripheral surface to the stent.

FIG. 8 shows a further embodiment of a stent in which there is a first ring 80, a second ring 82, a third ring 84 and a fourth ring 86. Between each pair of rings there is a zig zag strut portion 88. The stent according to this embodiment of the invention can be made from a single length of wire commencing with the loop 89 on the ring 80 and terminating with the loop 90 on the ring 86.

By this arrangement, a substantially cylindrical elongated stent can be formed without welds which could introduce weakness into the stent.

FIG. 9 shows an arrangement of bifurcated or branched stent graft according to this invention using a stent of the present invention.

The stent graft comprises a tubular main body 100 with well-known Gianturco type zig zag Z stents 102 along its length. Extending from a bifurcation 103 in the tubular body 100 is a side arm 104. The side arm 104 has a Gianturco type zig zag Z stent 105 and terminates in a ring stent 106 of the type disclosed in this invention. The use of the stent graft 106 on the side arm 104 provides a diametrically stable arm into which an extension leg or arm can be inserted with good reliability for sealing into the side arm either using a covered self expanding stent or a covered balloon expandable stent.

FIG. 10 shows a perspective view of a still further embodiment of a stent according to this invention. In this embodiment, the stent has two circles or turns of wire 109 starting with a loop 111 to form a ring assembly 110 of wire at its upper end and a number of zig zag struts 112 of wire extending axially from the circumference of the rings 110. In this embodiment, however, all of the pairs of struts 112 commence at the ring 110 and after six pairs of zig zag struts 112 a partial turn of wire 114 follows the ring 110 and terminates in a loop 116 to complete the stent. The stent of this embodiment may be particularly useful for mounting onto a leg or arm of a stent graft to provide dimensional stability at its end.

FIG. 11 and FIG. 12 show a further alternative embodiment of the invention.

FIG. 11 shows a stylised or developed view of a stent according to an embodiment of the invention laid out flat to show the continuous strand of Nitinol or stainless steel formed into the rings and struts. FIG. 12 shows the stent of FIG. 11 in a perspective view. In this embodiment there are in effect five sets of bends at each ring of the stent but there may be other odd numbers of sets of bends such as seven or nine.

The stent 120 of this embodiment has a single continuous length of material such as wire starting at loop 122 and forming a first ring 124 to a bend 126 and then a first angled strut 128 to another bend 130 and then into a second ring 132 which is spaced apart, essentially coaxial with and parallel to the first ring 124. The second ring 132 has one and one fifth turns and then a bend 134 and then an angled strut 136 to the first ring and a bend 138. Beyond the bend 138 there is a circumferential peripheral portion 140 essentially parallel and adjacent to the first ring 124 to a further bend 142. There are then alternate struts and peripheral portions with bends in between them of the continuous length of material making a total of ten struts in all ending with bend 144. After the bend 144 the continuous length of material extends in a circumferential peripheral portion 146 essentially parallel and adjacent to the first ring 124 to a terminal loop 148. It will be noted that by this arrangement there is at all portions of each ring at least two portions of the wire or other continuous material.

By the arrangement of this embodiment of the invention the sharp bends of the earlier embodiments between the zig zag struts do not exist and the short peripheral portions between bends become part of the ring and can be sutured to graft material making a more secure structure.

FIG. 13 shows a perspective view of the alternative embodiment of the invention. In this embodiment the stent 150 is formed from a tube or cannula of metal or other material and can be, for instance, laser cut from the tube or cannula in a known manner. The material of the stent 150 is resilient so that the stent is deformable.

The stent 150 includes a first resilient ring 152 and a second resilient ring 153 spaced apart axially from the first ring 152, and a plurality of diagonal or zig zag struts 154 around the periphery and between the first and second resilient rings. In this embodiment the struts 154 meet in between the first and second rings at 155 but in an alternative embodiment the struts may not cross between the first and second rings. FIG. 13 shows a squat ring stent according to the invention, that is, the height is about half the diameter.

FIG. 14 shows a perspective view of the alternative embodiment of the invention. In this embodiment the ring stent is formed from a tube or cannula of metal or other material and can be, for instance, laser cut from the tube or cannula in a known manner. The material of the stent 160 is resilient so that the stent is deformable.

The ring stent includes a first resilient ring 162 and a second resilient ring 163 spaced apart axially from the first ring 162, and a plurality of diagonal or zig zag struts 164 around the periphery and between the first and second resilient rings. The struts cross between the first ring 162 and second ring 163 to form junctions 165. In this embodiment the ring stent is tall rather than squat, that is, the height is about twice the diameter.

Throughout this specification various indications have been given as to the scope of the invention but the invention is not limited to any one of these but may reside in two or more combined together. The examples are given for illustration only and not for limitation. 

The invention claimed is:
 1. A wire stent assembly comprising: a first end having a periphery, a second end having a periphery, a longitudinal axis, a first resilient wire portion having a terminal end, a first section and a second section, the first section comprising a first planar ring disposed perpendicular to the longitudinal axis of the wire stent assembly and defining the periphery of the first end of the wire stent assembly, the first section having a first loop of wire at its terminal end that is perpendicular to the first planar ring and parallel to the longitudinal axis, the second section of wire of the first resilient wire portion comprising a length of the first resilient wire portion extending from the first loop of wire of the first section to the second end of the wire stent assembly and a second loop of wire adjacent the second end that is perpendicular to the first planar ring and parallel to the longitudinal axis, a second resilient wire portion having a terminal end, a first section and a second section, the first section comprising a second planar ring disposed perpendicular to the longitudinal axis of the wire stent assembly and defining the periphery of the second end of the wire stent assembly, the first section of wire of the second resilient wire portion having a first loop of wire at its terminal end that is perpendicular to the second planar ring and parallel to the longitudinal axis, the second section of wire of the second resilient wire portion comprising a length of the second resilient wire portion extending from the first loop of the first section of the second resilient wire portion toward the first end of the stent and a second loop of wire adjacent the first end of the wire stent assembly that is perpendicular to the second planar ring and parallel to the longitudinal axis, and wherein each of the first and second planar rings comprises at least one full turn of wire.
 2. The wire stent assembly of claim 1, wherein the first loop of the first section of the first resilient wire portion abuts the second planar ring.
 3. The wire stent assembly of claim 1, wherein the length of the second section of each of the first and resilient wire portions extend from the first end periphery to the second end periphery.
 4. The wire stent assembly of claim 1, wherein at least one of the second sections of the first and second wire portions are parallel to the longitudinal axis.
 5. The wire stent assembly of claim 1, wherein the second section of the first resilient wire portion is spaced radially away from the second section of the second resilient wire.
 6. A wire stent assembly comprising: a first end having a periphery, a second end having a periphery, a longitudinal axis, a first resilient wire portion having a terminal end, a first section and a second section, the first section comprising a first planar ring disposed perpendicular to the longitudinal axis of the wire stent assembly and defining the periphery of the first end of the wire stent assembly, the first section having a first loop of wire at its terminal end that is perpendicular to the first planar ring and parallel to the longitudinal axis, the second section of wire of the first resilient wire portion comprising a length of the first resilient wire portion extending from the first loop of wire of the first section to the second end of the wire stent assembly and a second loop of wire adjacent the second end that is perpendicular to the first planar ring and parallel to the longitudinal axis, a second resilient wire portion having a terminal end, a first section and a second section, the first section comprising a second planar ring disposed perpendicular to the longitudinal axis of the wire stent assembly and defining the periphery of the second end of the wire stent assembly, the first section of wire of the second resilient wire portion having a first loop of wire at its terminal end that is perpendicular to the second planar ring and parallel to the longitudinal axis, the second section of wire of the second resilient wire portion comprising a length of the second resilient wire portion extending from the first loop of the first section of the second resilient wire portion toward the first end of the stent and a second loop of wire adjacent the first end of the wire stent assembly that is perpendicular to the second planar ring and parallel to the longitudinal axis.
 7. The wire stent assembly of claim 6, wherein the length of the second section of each of the first and resilient wire portions extend from the first end periphery to the second end periphery.
 8. The wire stent assembly of claim 6, wherein each ring comprises at least one full turn of wire.
 9. The wire stent assembly of claim 6, wherein the second section of the first resilient wire portion is spaced radially away from the second section of the second resilient wire portion.
 10. The wire stent assembly of claim 6, wherein at least one of the second sections of the first and second wire assembly are parallel to the longitudinal axis.
 11. The wire stent assembly of claim 6 wherein each of the terminal ends of the first and second resilient wire portions lie within its loop.
 12. A stent graft comprising: a tube of graft material having a first end, a second end, a first opening at the first end having a periphery, a second opening at the second end having a periphery, and a longitudinal axis from the first end to the second end, a wire stent assembly attached to the tube of graft material, the wire stent assembly comprising: a first end, a second end, a longitudinal axis, a first resilient wire portion having a terminal end, a first section and a second section, the first section comprising a first planar ring disposed perpendicular to the longitudinal axes of the wire stent assembly and the tube of graft material and defining the periphery of the first end of the tube of graft material, the first section having a first loop of wire at its terminal end that is perpendicular to the first planar ring and parallel to the longitudinal axis, the second section of wire of the first resilient wire portion comprising a length of the first resilient wire portion extending from the first loop of wire of the first section to the second end of the wire stent assembly and a second loop of wire adjacent the second end of the wire stent assembly that is perpendicular to the first planar ring and parallel to the longitudinal axes of the tube of graft material and the wire stent assembly, a second resilient wire portion having a terminal end, a first section and a second section, the first section comprising a second planar ring disposed perpendicular to the longitudinal axes of the wire stent assembly and the tube of graft material and defining the periphery of the second end of the tube of graft material, the first section of wire of the second resilient wire portion having a first loop of wire at its terminal end that is perpendicular to the second planar ring and parallel to the longitudinal axes of the tube of graft material and the wire stent assembly, the second section of wire of the second resilient wire portion comprising a length of the second resilient wire portion extending from the first loop of the first section of the second resilient wire portion toward the first end of the wire stent assembly and a second loop of wire adjacent the first end of the wire stent assembly that is perpendicular to the second planar ring and parallel to the longitudinal axes of the tube of graft material and the wire stent assembly, wherein the first and second resilient wire portions are attached to the tube of graft material at the peripheries of the tube of graft material and at least partially along the lengths of the second sections of the first and second resilient wire portion to provide support for the tube of graft material.
 13. The wire stent assembly of claim 12, wherein the length of the second section of each of the first and resilient wire portions extend from the first end periphery to the second end periphery.
 14. The wire stent assembly of claim 12, wherein each ring comprises at least one full turn of wire.
 15. The wire stent assembly of claim 12, wherein the second section of the first resilient wire portion is spaced radially away from the second section of the second resilient wire portion.
 16. The wire stent assembly of claim 12, wherein at least one of the second sections of the first and second wire assembly are parallel to the longitudinal axis.
 17. The wire stent assembly of claim 12, wherein each of the terminal ends of the first and second resilient wire portions lie within a respective loop.
 18. The stent graft of claim 12, wherein the first ring is stitched about the periphery of the first open end and the second ring is stitched about the periphery of the second open end.
 19. The stent graft of claim 12, wherein the first loop of wire of the first resilient wire portion and the first loop of wire of the second resilient wire portion are closed loops.
 20. The stent graft of claim 12, wherein at least one of the second loops is configured to abut a ring. 